Literature DB >> 9832050

Severe primary pulmonary hypoplasia ("acinar dysplasia") in sibs: a genetically determined mesodermal defect?

P Moerman, C Vanhole, H Devlieger, J P Fryns.   

Abstract

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Year:  1998        PMID: 9832050      PMCID: PMC1051499          DOI: 10.1136/jmg.35.11.964

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  12 in total

1.  Congenital acinar aplasia: an extreme form of pulmonary maldevelopment.

Authors:  H M Chambers
Journal:  Pathology       Date:  1991-01       Impact factor: 5.306

2.  Acinar dysplasia: a new form of pulmonary maldevelopment.

Authors:  J C Rutledge; P Jensen
Journal:  Hum Pathol       Date:  1986-12       Impact factor: 3.466

3.  Mammalian lung development: interactions in formation and morphogenesis of tracheal buds.

Authors:  N K Wessells
Journal:  J Exp Zool       Date:  1970-12

Review 4.  Pathology of the lung in the fetus and neonate, with particular reference to problems of growth and maturation.

Authors:  J S Wigglesworth
Journal:  Histopathology       Date:  1987-07       Impact factor: 5.087

5.  Errors of morphogenesis: concepts and terms. Recommendations of an international working group.

Authors:  J Spranger; K Benirschke; J G Hall; W Lenz; R B Lowry; J M Opitz; L Pinsky; H G Schwarzacher; D W Smith
Journal:  J Pediatr       Date:  1982-01       Impact factor: 4.406

6.  Familial pulmonary hypoplasia.

Authors:  P Boylan; A Howe; J Gearty; N G O'Brien
Journal:  Ir J Med Sci       Date:  1977-06       Impact factor: 1.568

7.  Primary pulmonary hypoplasia in the neonate.

Authors:  L E Swischuk; C J Richardson; M M Nichols; M J Ingman
Journal:  J Pediatr       Date:  1979-10       Impact factor: 4.406

8.  Familial isolated pulmonary hypoplasia: a case report, suggesting autosomal recessive inheritance.

Authors:  B Frey; A Fleischhauer; M Gersbach
Journal:  Eur J Pediatr       Date:  1994-06       Impact factor: 3.183

9.  Primary pulmonary hypoplasia: report of a case with polyhydramnios.

Authors:  G Mendelsohn; G M Hutchins
Journal:  Am J Dis Child       Date:  1977-11

10.  The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary.

Authors:  S Kimura; Y Hara; T Pineau; P Fernandez-Salguero; C H Fox; J M Ward; F J Gonzalez
Journal:  Genes Dev       Date:  1996-01-01       Impact factor: 11.361

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  6 in total

1.  Imaging of primary unilateral pulmonary hypoplasia: a case report.

Authors:  P Demaret; R Menten; C Debauche; S Moniotte
Journal:  Eur J Pediatr       Date:  2008-12-09       Impact factor: 3.183

Review 2.  Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental Disorders.

Authors:  Marie Vincent; Justyna A Karolak; Gail Deutsch; Tomasz Gambin; Edwina Popek; Bertrand Isidor; Przemyslaw Szafranski; Cedric Le Caignec; Paweł Stankiewicz
Journal:  Am J Respir Crit Care Med       Date:  2019-11-01       Impact factor: 21.405

3.  Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.

Authors:  Justyna A Karolak; Marie Vincent; Gail Deutsch; Tomasz Gambin; Benjamin Cogné; Olivier Pichon; Francesco Vetrini; Heather C Mefford; Jennifer N Dines; Katie Golden-Grant; Katrina Dipple; Amanda S Freed; Kathleen A Leppig; Megan Dishop; David Mowat; Bruce Bennetts; Andrew J Gifford; Martin A Weber; Anna F Lee; Cornelius F Boerkoel; Tina M Bartell; Catherine Ward-Melver; Thomas Besnard; Florence Petit; Iben Bache; Zeynep Tümer; Marie Denis-Musquer; Madeleine Joubert; Jelena Martinovic; Claire Bénéteau; Arnaud Molin; Dominique Carles; Gwenaelle André; Eric Bieth; Nicolas Chassaing; Louise Devisme; Lara Chalabreysse; Laurent Pasquier; Véronique Secq; Massimiliano Don; Maria Orsaria; Chantal Missirian; Jérémie Mortreux; Damien Sanlaville; Linda Pons; Sébastien Küry; Stéphane Bézieau; Jean-Michel Liet; Nicolas Joram; Tiphaine Bihouée; Daryl A Scott; Chester W Brown; Fernando Scaglia; Anne Chun-Hui Tsai; Dorothy K Grange; John A Phillips; Jean P Pfotenhauer; Shalini N Jhangiani; Claudia G Gonzaga-Jauregui; Wendy K Chung; Galen M Schauer; Mark H Lipson; Catherine L Mercer; Arie van Haeringen; Qian Liu; Edwina Popek; Zeynep H Coban Akdemir; James R Lupski; Przemyslaw Szafranski; Bertrand Isidor; Cedric Le Caignec; Paweł Stankiewicz
Journal:  Am J Hum Genet       Date:  2019-01-10       Impact factor: 11.025

4.  Primary alveolar capillary dysplasia (acinar dysplasia) and surfactant protein B deficiency: a clinical, radiological and pathological study.

Authors:  Claes O Hugosson; Husam M Salama; Fouad Al-Dayel; Nuha Khoumais; Abdul H Kattan
Journal:  Pediatr Radiol       Date:  2004-10-14

Review 5.  Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects.

Authors:  Hiroshi Kitazawa; Shigeo Kure
Journal:  Clin Med Insights Circ Respir Pulm Med       Date:  2015-10-11

6.  Congenital acinar dysplasia: report of a case and review of literature.

Authors:  Mary Langenstroer; S J Carlan; Naim Fanaian; Suzanna Attia
Journal:  AJP Rep       Date:  2012-12-10
  6 in total

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